FAM13B1 Rabbit anti-Human, Polyclonal, Bioss

Catalog No.	Quantity
50-198-6778	100 μL

Catalog No. 50-198-6778 Supplier Bioss Supplier No. BS5757R

Description

Rabbit Polyclonal Antibody

FAM13B is a 915 amino acid protein that is encoded by a gene that maps to human chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6% of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

Specifications

• Antigen: FAM13B1
• Applications: Immunofluorescence, Immunohistochemistry (Paraffin), Western Blot
• Classification: Polyclonal
• Concentration: 1 μg/mL
• Conjugate: Unconjugated
• Formulation: PBS with 1% BSA, 50% glycerol and 0.09% sodium azide; pH
• Gene: FAM13B
• Gene Accession No.: Q9NYF5
• Gene Alias: 2610024E20Rik; ARHGAP49; AW060714; AW546153; C5orf5; Fam13b; FAM13B1; family with sequence similarity 13 member B; family with sequence similarity 13, member B; family with sequence similarity 13, member B1; GAP-like protein N61; KHCHP; N61; Protein FAM13B
• Gene Symbols: FAM13B
• Host Species: Rabbit
• Immunogen: KLH conjugated synthetic peptide derived from human FAM13B1.
• Purification Method: Protein A
• Quantity: 100 μL
• Regulatory Status: RUO
• Primary or Secondary: Primary
• Gene ID (Entrez): 51306
• Target Species: Human
• Content And Storage: -20°C
• Product Type: Antibody
• Form: Liquid
• Isotype: IgG